跳至主要内容
临床试验/NL-OMON47021
NL-OMON47021已完成不适用

Diagnostic accuracy of spectral computed tomography for detection of flow limiting coronary stenosis using fractional flow reserve as the standard of reference - CLARITY study

niversitair Medisch Centrum Utrecht0 个研究点目标入组 75 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
75

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • - >=18 years old;
  • - Suspected or known stable angina with pre-test likelihood of 50-85% using the method recommended by the European Society of Cardiology 2013 Guidelines on the management of stable coronary artery disease (Eur Heart J 2013);
  • - Referred for invasive testing with fractional flow reserve;
  • - Willing and able to give informed consent.

排除标准

  • - Subjects with suspected or known stable angina with pre-test likelihood of 0-50% using the method recommended by the European Society of Cardiology 2013 Guidelines on the management of stable coronary artery disease (Eur Heart J 2013);
  • - Subjects who because of age, general medical or psychiatric condition, or physiologic status cannot give valid informed consent or tolerate the coronary CTA examination;
  • - Subjects with (severe) renal insufficiency, indicated as glomerular filtration rate (GFR) <60 ml/min;
  • - Subjects with unknown GFR or obtained >3 months before the planned scan;
  • - Contraindication or allergy to intravenous contrast agent(s);
  • - Subjects who participate in an other study with radiation which is estimated to be in risk category III (ICRP 62);
  • - Subjects who are pregnant;
  • - Subjects with contraindications to cardiac CT and/or step and shoot protocol, betablockers, adenosine or nitroglycerine.

研究者

发起方
niversitair Medisch Centrum Utrecht

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